Evidence map›Paper›PMID 33134810›Full record

ArticleRheumatology advances in practice2020

An open-label, randomized controlled trial of sulfamethoxazole-trimethoprim for

Masako Utsunomiya, Hiroaki Dobashi, Toshio Odani, Kazuyoshi Saito, Naoto Yokogawa, Kenji Nagasaka, Kenchi Takenaka, Makoto Soejima, Takahiko Sugihara, Hiroyuki Hagiyama and 16 more

Abstract read
In one paragraph

Article in Rheumatology advances in practice, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 3 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trimethoprim-Sulfamethoxazole (Bactrim) Dose Optimization inInternational journal of environmental research and public health · 2022
    Pooled it
  4. Model-Based Evaluation of the Warfarin-Sulfamethoxazole Drug-Drug Interaction.European journal of drug metabolism and pharmacokinetics · 2026
    Article
  5. Article
  6. Article
  7. Observational
  8. Low-dose atovaquone for prophylaxis ofEULAR rheumatology open · 2025
    Article
  9. T-cell subsets inClinical & translational immunology · 2025
    Review
  10. Low-Dose Sulfamethoxazole-Trimethoprim Could PreventTherapeutics and clinical risk management · 2025
    Article
  11. Article
  12. Review
  13. Clinical microbiology reviews · 2024
    Review
  14. Article
  15. Observational
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

26 authors.

Masako UtsunomiyaDepartment of Rheumatic Diseases, Tokyo Metropolitan Tama Medical Center, Fuchu, Tokyo.
Hiroaki DobashiDivision of Hematology, Rheumatology and Respiratory Medicine, Department of Internal Medicine, Faculty of Medicine, Kagawa University, Kida-gun, Kagawa.
Toshio OdaniThird Department of Internal Medicine, Obihiro-Kosei General Hospital, Obihiro, Hokkaido.
Kazuyoshi SaitoFirst Department of Internal Medicine, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Fukuoka.
Naoto YokogawaDepartment of Rheumatic Diseases, Tokyo Metropolitan Tama Medical Center, Fuchu, Tokyo.
Kenji NagasakaDepartments of Pharmacovigilance.
Kenchi TakenakaRheumatology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo.ORCID 0000-0002-2206-4844
Makoto SoejimaDepartment of Rheumatology, Ome Municipal General Hospital, Ome, Tokyo.
Takahiko SugiharaDepartment of Medicine and Rheumatology, Tokyo Metropolitan Geriatric Hospital, Tokyo.
Hiroyuki HagiyamaDepartment of Rheumatology, Yokohama City Minato Red Cross Hospital, Yokohama, Kanagawa.
Shinya HirataDepartment of Hematology, Rheumatology, and Infectious Disease, Kumamoto University Graduate School of Medicine, Kumamoto, Kumamoto.
Kazuo MatsuiDepartment of Rheumatology, Kameda Medical Center, Kamogawa, Chiba.
Yoshinori NonomuraDepartment of Rheumatology, Tokyo Kyosai Hospital, Tokyo.
Masahiro KondoDepartment of Rheumatology, Faculty of Medicine, Shimane University, Izumo, Shimane.
Fumihito SuzukiDepartment of Rheumatology, Soka Municipal Hospital, Soka, Saitama.
Yasushi NawataCenter for Rheumatic Disease, Chibaken Saiseikai Narashino Hospital, Narashino, Chiba.
Makoto TomitaClinical Research Center, Medical Hospital of Tokyo Medical and Dental University.
Mari KiharaDepartments of Pharmacovigilance.
Waka Yokoyama-KokuryoDepartments of Pharmacovigilance.
Fumio HiranoDepartments of Pharmacovigilance.ORCID 0000-0002-5169-0692
Hayato YamazakiDepartments of Pharmacovigilance.
Ryoko SakaiDepartments of Pharmacovigilance.
Toshihiro NankiDepartments of Pharmacovigilance.
Ryuji KoikeDepartments of Pharmacovigilance.
Nobuyuki MiyasakaRheumatology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo.
Masayoshi HarigaiDepartments of Pharmacovigilance.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe aim was to investigate the long-term prophylactic efficacy, drug retention and safety of low-dose sulfamethoxazole-trimethoprim (SMX/TMP) prophylaxis against

methodsAdult patients with rheumatic diseases receiving prednisolone ≥0.6 mg/kg/day were randomized into the single-strength group (SS; SMX/TMP 400/80 mg daily), the half-strength group (HS; 200/40 mg daily) or the escalation group (ES; starting at 40/8 mg and increasing incrementally to 200/40 mg daily) and treated for 24 weeks, then observed for 52 weeks. The primary endpoint, the PCP non-incidence rate (non-IR) at week 24, has been reported previously. The secondary endpoints were the PCP non-IR at week 52, treatment discontinuation rate and adverse events.

resultsFifty-eight, 59 and 55 patients in the SS, HS and ES, respectively, received SMX/TMP. PCP did not develop in any of the patients by week 52. The estimated PCP non-IR in patients receiving SMX/TMP 200/40 mg daily (HS and ES) was 96.8-100%. Throughout the 52-week observation period, the overall discontinuation rate was significantly lower in HS than in SS (22.7

conclusionSMX/TMP 200/40 mg had a high PCP prevention rate and was superior to SMX/TMP 400/80 mg in terms of drug retention and safety.

trial registrationUniversity Hospital Medical Information Network Clinical Trials Registry, UMIN000007727.

Indexed as

drug discontinuation rateefficacyPneumocystis pneumoniaprophylaxisrandomized controlled trialrheumatic diseasesafetysulfamethoxazole–trimethoprim

Identifiers

PMID33134810
PMCPMC7585401

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.